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- Which of the following carbocations would be expected to rearrange? None of these would be expected to rearrange. „CH3 CH;CCH,CH3 ČH3 .CH3 „CH3In light of your answer to Problem 11-74, explain why one of the following isomers undergoes E2 reaction approximately 100 times as fast as the other. Which isomer is more reactive, and why?Which carbocation below is/are the most stable one? Circle it (them)
- For the following reactions, fill in the boxes with the starting material that leads to the predominant product or products.4. Rank the following carbocations according to stability (1: most stable, 5: least stable.). ht t tá OCH 3 +What is the expected major product for the following reaction? 1. Hg(OAc)2, H₂O 2. NaBH4, NaOH OH HO ? OH ㅎ... HO HO 11 III O IV OV + enantiomer || + enantiomer III IV V
- Draw a structural formula for the major organic product of the reaction shown below. C(CH3)3 CH2 + ether H3O + CuLi H3C 2 • You do not have to consider stereochemistry. + - 4 √n [ ? ChemDoodle ⓇKl117.The cis and trans 2-butene stereoisomers have the following rate constant values associated with the electrophilic addition of water in an acid medium at the same temperature. what is the difference between the two values through the energy profile of each reaction. CH3 H,O productos H+ H3C k = 3.51 x 10- M's1 H3C CH3 H,0 > productos H+ k = 8.32 x 10®M's1
